首页> 美国卫生研究院文献>The EMBO Journal >Xenopus laevis U1 snRNA genes: characterisation of transcriptionally active genes reveals major and minor repeated gene families.
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Xenopus laevis U1 snRNA genes: characterisation of transcriptionally active genes reveals major and minor repeated gene families.

机译:非洲爪蟾U1 snRNA基因:转录活性基因的表征揭示了主要和次要重复的基因家族。

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摘要

Xenopus laevis U1 snRNA genes are found in several different genomic arrangements. The major family of genes is organised in tandem repeats of 1.8 kb. The minor U1-family is much less abundant and is present on 1.2-kb HinfI restriction fragments. In addition there are genomic arrangements present in one or very few copies, which could represent the ends of repeating units. There is no evidence for the presence of U1 pseudogenes in Xenopus. A cluster of U1 snRNA genes consisting of a member of the minor class of U1 snRNA genes and two of the 'rarely represented' genes was cloned. All three genes were expressed upon microinjection into frog oocytes. A fragment containing 149 bp of 5' flanking sequence, the RNA coding sequence, and 27 bp of 3' flanking sequence was shown to be accurately transcribed into U1 snRNA. These oocyte transcripts are assembled into specific U1 snRNPs. Sequence comparison of the regions flanking Xenopus U1 and U2 snRNA genes showed the presence of two blocks of homology, which are also conserved in many other U snRNA genes. One of these blocks is found at position -60 to -50 before the coding sequence, and we discuss its possible role in the correct initiation of transcription. The other is 3' to the coding sequence and may be involved in the accurate production of mature 3' ends in the RNA.
机译:非洲爪蟾U1 snRNA基因存在于几种不同的基因组排列中。主要基因家族以1.8 kb的串联重复序列组织。较小的U1族的数量要少得多,并且存在于1.2kb HinfI限制性片段上。另外,基因组安排存在一个或很少的副本中,这可能代表重复单元的末端。没有证据表明非洲爪蟾中存在U1假基因。克隆了由U1 snRNA基因的一小部分成员和两个“罕见代表”基因组成的U1 snRNA基因簇。所有三个基因在显微注射到青蛙卵母细胞中表达。含有149 bp的5'侧翼序列,RNA编码序列和27 bp的3'侧翼序列的片段已被正确转录为U1 snRNA。这些卵母细胞转录本组装成特定的U1 snRNPs。 Xenopus U1和U2 snRNA基因两侧区域的序列比较显示,存在两个同源性模块,这在许多其他U snRNA基因中也保守。在编码序列之前的-60至-50之间发现了这些嵌段之一,我们讨论了其在正确转录起始中的可能作用。另一个是编码序列的3'端,可能与RNA中成熟3'端的准确产生有关。

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